Human immune response to streptococcal inhibitor of complement, a serotype M1 group A Streptococcus extracellular protein involved in epidemics

被引:33
作者
Hoe, NP
Kordari, P
Cole, R
Liu, MY
Palzkill, T
Huang, WZ
McLellan, D
Adams, GJ
Hu, M
Vuopio-Varkila, J
Cate, TR
Pichichero, ME
Edwards, KM
Eskola, J
Low, DE
Musser, JM
机构
[1] NIAID, Lab Human Bacterial Pathogenesis, Rocky Mt Labs, NIH, Hamilton, MT 59840 USA
[2] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Microbiol & Immunol, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[5] Vet Affairs Res Serv, Memphis, TN USA
[6] Univ Tennessee, Dept Med, Memphis, TN 38104 USA
[7] Vanderbilt Univ, Sch Med, Dept Pediat, Div Infect Dis, Nashville, TN 37212 USA
[8] ID Vaccine Corp, Bothell, WA USA
[9] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[10] Natl Publ Hlth Inst, Dept Bacteriol, Helsinki, Finland
[11] Natl Publ Hlth Inst, Dept Vaccines, Helsinki, Finland
[12] Mt Sinai Hosp, Dept Microbiol, Toronto, ON M5G 1X5, Canada
[13] Univ Toronto, Toronto, ON, Canada
关键词
D O I
10.1086/315882
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Streptococcal inhibitor of complement (Sic) is a highly polymorphic extracellular protein made by serotype M1 group A Streptococcus strains that contributes to bacterial persistence in the mammalian upper respiratory tract. New variants of the Sic protein arise very rapidly by positive selection in human populations during M1 epidemics. The human antibody response to Sic was analyzed, Of 636 persons living in diverse localities, 43% had anti-Sic serum antibodies, but only 16.4% had anti-M1 protein serum antibody. Anti-Sie antibody was also present in nasal wash specimens in high frequency. Linear B cell epitope mapping showed that serum antibodies recognized epitopes located in structurally variable regions of Sic and the amino terminal hypervariable region of the M1 protein. Phage display analyses confirmed that the polymorphic regions of Sic are primary targets of host antibodies. These results support the hypothesis that selection of Sic variants occurs on mucosal surfaces by a mechanism that involves acquired host antibody.
引用
收藏
页码:1425 / 1436
页数:12
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